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临床试验/jRCT1030260046
jRCT1030260046招募中不适用

Sex-Dependent Effects of Acute Normobaric Hypoxia on Dynamic Cerebral Autoregulation

未提供0 个研究点目标入组 40 人开始时间: 待定
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized

入排标准

年龄范围
18age old over 至 35age old under(—)
性别
All

入选标准

  • Individuals aged 18 to 35 years at the time of obtaining informed consent
  • Individuals who have received a thorough explanation regarding participation in this study and have provided voluntary consent based on full understanding
  • Individuals confirmed to be in good health based on medical interview and health examination results
  • Females with a normal menstrual cycle length (25-38 days)
  • Individuals in whom stable cerebral blood flow velocity waveforms can be obtained by transcranial Doppler ultrasonography in the supine resting position

排除标准

  • Individuals from whom consent to participate in the study could not be obtained
  • Individuals with, or with a history of, cardiovascular disease (including hypertension and arrhythmia), neurological disease (including cerebrovascular disease and epilepsy), respiratory disease (including bronchial asthma and COPD), autonomic nervous system dysfunction, or severe systemic disease; and individuals with anemia that has not improved with treatment
  • Individuals who show any of the following findings on screening examination (blood pressure measurement and electrocardiography): systolic blood pressure >=140 mmHg or diastolic blood pressure >=90 mmHg, or electrocardiographic abnormalities such as atrial fibrillation, atrial flutter, or frequent premature contractions
  • Individuals with a history of allergy or skin reactions to ultrasound gel
  • Females who regularly use hormonal agents such as oral contraceptives, those with irregular menstrual cycles, or those who are pregnant
  • Females for whom it is determined that scheduling the experiment during the follicular phase of the menstrual cycle is not feasible
  • Individuals deemed inappropriate as study participants by the principal investigator

研究者

发起方
未提供

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